CAYMAN CHEMICAL COMPANY Non-Antibody Products — page 647 of 674
Non-Antibody Products
Page 647 of 674
| Name | Description | Size | Catalog # | |
|---|---|---|---|---|
| ULK-101 | A ULK1 and ULK2 inhibitor (IC50s = 8.3 and 30 nM, respectively); selective… | 25 mg | 40403-25 | More Info |
| ULK-101 | A ULK1 and ULK2 inhibitor (IC50s = 8.3 and 30 nM, respectively); selective… | 5 mg | 40403-5 | More Info |
| UltraPure LPS from Escherichia coli O111:B4 | A form of LPS extracted from wild-type S-form E. coli serotype O111:B4 and… | 1 mg | 28872-1 | More Info |
| UltraPure Water | Water used for the preparation of ELISA reagents and buffers | 1 L | 400000-1 | More Info |
| UM-164 | An inhibitor of Src and p38 MAPK kinases (Kds = 2.7, 2.2, and 5.5 nM for c… | 1 mg | 26188-1 | More Info |
| UM-164 | An inhibitor of Src and p38 MAPK kinases (Kds = 2.7, 2.2, and 5.5 nM for c… | 10 mg | 26188-10 | More Info |
| UM-164 | An inhibitor of Src and p38 MAPK kinases (Kds = 2.7, 2.2, and 5.5 nM for c… | 25 mg | 26188-25 | More Info |
| UM-164 | An inhibitor of Src and p38 MAPK kinases (Kds = 2.7, 2.2, and 5.5 nM for c… | 5 mg | 26188-5 | More Info |
| U-99194 (maleate) | A dopamine D3 receptor antagonist (Ki = 160 nM for the human receptor); se… | 10 mg | 35854-10 | More Info |
| U-99194 (maleate) | A dopamine D3 receptor antagonist (Ki = 160 nM for the human receptor); se… | 25 mg | 35854-25 | More Info |
| U-99194 (maleate) | A dopamine D3 receptor antagonist (Ki = 160 nM for the human receptor); se… | 5 mg | 35854-5 | More Info |
| U-99194 (maleate) | A dopamine D3 receptor antagonist (Ki = 160 nM for the human receptor); se… | 50 mg | 35854-50 | More Info |
| UMB-32 | An inhibitor of BRD4 (Kd = 550 nM; IC50 = 637 nM),TAF1 (Kd = 560 nM), and… | 1 mg | 17123-1 | More Info |
| UMB-32 | An inhibitor of BRD4 (Kd = 550 nM; IC50 = 637 nM),TAF1 (Kd = 560 nM), and… | 10 mg | 17123-10 | More Info |
| UMB-32 | An inhibitor of BRD4 (Kd = 550 nM; IC50 = 637 nM),TAF1 (Kd = 560 nM), and… | 25 mg | 17123-25 | More Info |
| UMB-32 | An inhibitor of BRD4 (Kd = 550 nM; IC50 = 637 nM),TAF1 (Kd = 560 nM), and… | 5 mg | 17123-5 | More Info |
| Umbelliferone | A derivative and metabolite of coumarin with diverse biological activities… | 100 mg | 24665-100 | More Info |
| Umbelliferone | A derivative and metabolite of coumarin with diverse biological activities… | 25 mg | 24665-25 | More Info |
| Umbelliferone | A derivative and metabolite of coumarin with diverse biological activities… | 50 mg | 24665-50 | More Info |
| Umbelliprenin | A prenylated coumarin with diverse biological activities; inhibits 5-LO in… | 1 mg | 27894-1 | More Info |
| Umbelliprenin | A prenylated coumarin with diverse biological activities; inhibits 5-LO in… | 10 mg | 27894-10 | More Info |
| Umbelliprenin | A prenylated coumarin with diverse biological activities; inhibits 5-LO in… | 25 mg | 27894-25 | More Info |
| Umbelliprenin | A prenylated coumarin with diverse biological activities; inhibits 5-LO in… | 5 mg | 27894-5 | More Info |
| Umeclidinium (bromide) | A muscarinic acetylcholine receptor antagonist (Kis = 0.05-0.16 nM for M1-… | 10 mg | 20700-10 | More Info |
| Umeclidinium (bromide) | A muscarinic acetylcholine receptor antagonist (Kis = 0.05-0.16 nM for M1-… | 100 mg | 20700-100 | More Info |
| Umeclidinium (bromide) | A muscarinic acetylcholine receptor antagonist (Kis = 0.05-0.16 nM for M1-… | 50 mg | 20700-50 | More Info |
| U-62066 (mesylate) | An analytical reference standard categorized as an opioid; intended for re… | 1 mg | 25072-1 | More Info |
| U-62066 (mesylate) | An analytical reference standard categorized as an opioid; intended for re… | 5 mg | 25072-5 | More Info |
| UMI-77 | A selective Mcl-1 inhibitor (Ki = 490 nM) that disrupts the heterodimeriza… | 1 mg | 19148-1 | More Info |
| UMI-77 | A selective Mcl-1 inhibitor (Ki = 490 nM) that disrupts the heterodimeriza… | 10 mg | 19148-10 | More Info |
| UMI-77 | A selective Mcl-1 inhibitor (Ki = 490 nM) that disrupts the heterodimeriza… | 5 mg | 19148-5 | More Info |
| Umifenovir-d6 (hydrochloride) | An internal standard for the quantification of arbidol by GC- or LC-MS | 1 mg | 31494-1 | More Info |
| Umifenovir-d6 (hydrochloride) | An internal standard for the quantification of arbidol by GC- or LC-MS | 5 mg | 31494-5 | More Info |
| Umifenovir-d6 (hydrochloride) | An internal standard for the quantification of arbidol by GC- or LC-MS | 500 µg | 31494-500 | More Info |
| Umifenovir (hydrochloride) | A broad-spectrum antiviral agent; inhibits the replication of H5N1 influen… | 10 mg | 16933-10 | More Info |
| Umifenovir (hydrochloride) | A broad-spectrum antiviral agent; inhibits the replication of H5N1 influen… | 100 mg | 16933-100 | More Info |
| Umifenovir (hydrochloride) | A broad-spectrum antiviral agent; inhibits the replication of H5N1 influen… | 5 mg | 16933-5 | More Info |
| Umifenovir (hydrochloride) | A broad-spectrum antiviral agent; inhibits the replication of H5N1 influen… | 50 mg | 16933-50 | More Info |
| Umirolimus | A rapamycin derivative; has immunosuppressive and anti-inflammatory effect… | 1 mg | 23585-1 | More Info |
| Umirolimus | A rapamycin derivative; has immunosuppressive and anti-inflammatory effect… | 5 mg | 23585-5 | More Info |
| Unacylated Ghrelin (dog) Easy Sampling EIA Kit | For the measurement of unacylated ghrelin | 96 Well | 501200-96 | More Info |
| Unacylated Ghrelin (human) Easy Sampling EIA Kit | For the measurement of unacylated ghrelin | 96 Well | 501190-96 | More Info |
| Unacylated Ghrelin (mouse, rat) Easy Sampling EIA Kit | For the measurement of unacylated ghrelin | 96 Well | 501180-96 | More Info |
| Unacylated Ghrelin (mouse, rat) Express EIA Kit | Ghrelin is an endogenous ligand for the growth hormone secretagogue recept… | 96 Well | 10008953-96 | More Info |
| Unacylated Ghrelin (pig) EIA Kit | For the measurement of unacylated ghrelin | 96 Well | 501230-96 | More Info |
| UNBS5162 | An antagonist of CXCL chemokine expression; demonstrates antiangiogenic pr… | 10 mg | 17739-10 | More Info |
| UNBS5162 | An antagonist of CXCL chemokine expression; demonstrates antiangiogenic pr… | 25 mg | 17739-25 | More Info |
| UNBS5162 | An antagonist of CXCL chemokine expression; demonstrates antiangiogenic pr… | 5 mg | 17739-5 | More Info |
| UNBS5162 | An antagonist of CXCL chemokine expression; demonstrates antiangiogenic pr… | 50 mg | 17739-50 | More Info |
| UNC0064-12 | A multi-kinase inhibitor; has been used as an affinity ligand for proteomi… | 1 mg | 33555-1 | More Info |
| UNC0064-12 | A multi-kinase inhibitor; has been used as an affinity ligand for proteomi… | 10 mg | 33555-10 | More Info |
| UNC0064-12 | A multi-kinase inhibitor; has been used as an affinity ligand for proteomi… | 25 mg | 33555-25 | More Info |
| UNC0064-12 | A multi-kinase inhibitor; has been used as an affinity ligand for proteomi… | 5 mg | 33555-5 | More Info |
| UNC0224 | A potent and selective G9a HMTase inhibitor (IC50 = 15 nM, Kd = 23 mM); mo… | 1 mg | 13631-1 | More Info |
| UNC0224 | A potent and selective G9a HMTase inhibitor (IC50 = 15 nM, Kd = 23 mM); mo… | 10 mg | 13631-10 | More Info |
| UNC0224 | A potent and selective G9a HMTase inhibitor (IC50 = 15 nM, Kd = 23 mM); mo… | 5 mg | 13631-5 | More Info |
| UNC0224 | A potent and selective G9a HMTase inhibitor (IC50 = 15 nM, Kd = 23 mM); mo… | 50 mg | 13631-50 | More Info |
| UNC0379 | A selective inhibitor of the lysine methyltransferase SET8 (IC50 = 7.3 &mi… | 10 mg | 16400-10 | More Info |
| UNC0379 | A selective inhibitor of the lysine methyltransferase SET8 (IC50 = 7.3 &mi… | 25 mg | 16400-25 | More Info |
| UNC0379 | A selective inhibitor of the lysine methyltransferase SET8 (IC50 = 7.3 &mi… | 5 mg | 16400-5 | More Info |
| UNC0631 | A potent and selective inhibitor of G9a activity in vitro (IC50 = 4 nM) an… | 1 mg | 11084-1 | More Info |
| UNC0631 | A potent and selective inhibitor of G9a activity in vitro (IC50 = 4 nM) an… | 10 mg | 11084-10 | More Info |
| UNC0631 | A potent and selective inhibitor of G9a activity in vitro (IC50 = 4 nM) an… | 25 mg | 11084-25 | More Info |
| UNC0631 | A potent and selective inhibitor of G9a activity in vitro (IC50 = 4 nM) an… | 5 mg | 11084-5 | More Info |
| UNC0638 | A potent, selective G9a and GLP HMTase inhibitor (IC50s = MB231 cells (IC5… | 1 mg | 10734-1 | More Info |
| UNC0638 | A potent, selective G9a and GLP HMTase inhibitor (IC50s = MB231 cells (IC5… | 10 mg | 10734-10 | More Info |
| UNC0638 | A potent, selective G9a and GLP HMTase inhibitor (IC50s = MB231 cells (IC5… | 5 mg | 10734-5 | More Info |
| UNC0638 | A potent, selective G9a and GLP HMTase inhibitor (IC50s = MB231 cells (IC5… | 50 mg | 10734-50 | More Info |
| UNC0642 | A selective inhibitor of G9a and GLP methyltransferases that competitively… | 1 mg | 14604-1 | More Info |
| UNC0642 | A selective inhibitor of G9a and GLP methyltransferases that competitively… | 10 mg | 14604-10 | More Info |
| UNC0642 | A selective inhibitor of G9a and GLP methyltransferases that competitively… | 5 mg | 14604-5 | More Info |
| UNC0646 | A potent and selective inhibitor of G9a and GLP activities in vitro (IC50s… | 1 mg | 11085-1 | More Info |
| UNC0646 | A potent and selective inhibitor of G9a and GLP activities in vitro (IC50s… | 10 mg | 11085-10 | More Info |
| UNC0646 | A potent and selective inhibitor of G9a and GLP activities in vitro (IC50s… | 5 mg | 11085-5 | More Info |
| UNC0646 | A potent and selective inhibitor of G9a and GLP activities in vitro (IC50s… | 50 mg | 11085-50 | More Info |
| UNC1079 | An inactive analog of UNC1215 intended for use as a negative control | 1 mg | 20566-1 | More Info |
| UNC1079 | An inactive analog of UNC1215 intended for use as a negative control | 10 mg | 20566-10 | More Info |
| UNC1079 | An inactive analog of UNC1215 intended for use as a negative control | 25 mg | 20566-25 | More Info |
| UNC1079 | An inactive analog of UNC1215 intended for use as a negative control | 5 mg | 20566-5 | More Info |
| UNC1215 | A potent, selective chemical probe for the methyl lysine reading function… | 1 mg | 13968-1 | More Info |
| UNC1215 | A potent, selective chemical probe for the methyl lysine reading function… | 10 mg | 13968-10 | More Info |
| UNC1215 | A potent, selective chemical probe for the methyl lysine reading function… | 5 mg | 13968-5 | More Info |
| UNC1215 | A potent, selective chemical probe for the methyl lysine reading function… | 50 mg | 13968-50 | More Info |
| UNC1999 | A selective, cell-permeable EZH2 inhibitor (IC50 = 2 nM) that has been sho… | 1 mg | 14621-1 | More Info |
| UNC1999 | A selective, cell-permeable EZH2 inhibitor (IC50 = 2 nM) that has been sho… | 10 mg | 14621-10 | More Info |
| UNC1999 | A selective, cell-permeable EZH2 inhibitor (IC50 = 2 nM) that has been sho… | 5 mg | 14621-5 | More Info |
| UNC1999 | A selective, cell-permeable EZH2 inhibitor (IC50 = 2 nM) that has been sho… | 50 mg | 14621-50 | More Info |
| UNC2025 | A potent, orally bioavailable inhibitor of the tyrosine kinases Mer and Fl… | 10 mg | 16613-10 | More Info |
| UNC2025 | A potent, orally bioavailable inhibitor of the tyrosine kinases Mer and Fl… | 25 mg | 16613-25 | More Info |
| UNC2025 | A potent, orally bioavailable inhibitor of the tyrosine kinases Mer and Fl… | 5 mg | 16613-5 | More Info |
| UNC2025 | A potent, orally bioavailable inhibitor of the tyrosine kinases Mer and Fl… | 50 mg | 16613-50 | More Info |
| UNC2250 | A selective inhibitor of Mer kinase activity, blocking the steady-state ph… | 1 mg | 17703-1 | More Info |
| UNC2250 | A selective inhibitor of Mer kinase activity, blocking the steady-state ph… | 10 mg | 17703-10 | More Info |
| UNC2250 | A selective inhibitor of Mer kinase activity, blocking the steady-state ph… | 5 mg | 17703-5 | More Info |
| UNC2250 | A selective inhibitor of Mer kinase activity, blocking the steady-state ph… | 50 mg | 17703-50 | More Info |
| UNC2327 | An allosteric inhibitor of PRMT3 (IC50 = 230 nM) | 1 mg | 18122-1 | More Info |
| UNC2327 | An allosteric inhibitor of PRMT3 (IC50 = 230 nM) | 10 mg | 18122-10 | More Info |
| UNC2327 | An allosteric inhibitor of PRMT3 (IC50 = 230 nM) | 25 mg | 18122-25 | More Info |
| UNC2327 | An allosteric inhibitor of PRMT3 (IC50 = 230 nM) | 5 mg | 18122-5 | More Info |
| UNC2881 | An inhibitor of Mer kinase (IC50 = 4.3 nM); selective for Mer over Axl and… | 10 mg | 29012-10 | More Info |
CAYMAN CHEMICAL COMPANY
CAYMAN CHEMICAL COMPANY
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Ann Arbor MI 48108
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